Polymer Nucleation under High-Driving Force, Long-Chain Conditions: Heat Release and the Separation of Timescales

2019 ◽  
Author(s):  
Kyle Hall ◽  
Simona Percec ◽  
Michael Klein

This study reveals important features of polymer crystal formation at high-driving forces in entangled polymer melts based on simulations of polyethylene. First and in contrast to small-molecule crystallization, the heat released during polymer crystallization does not appreciably influence structural details of early-stage, crystalline clusters (crystal nuclei). Second, early-stage polymer crystallization (crystal nucleation) can occur without substantial chain-level relaxation and conformational changes. This study's results indicate that local structures and environments guide crystal nucleation in entangled polymer melts under high-driving force conditions. Given that such conditions are often used to process polyethylene, local structures and the separation of timescales associated with crystallization and chain-level processes are anticipated to be of substantial importance to processing strategies. This study highlights new research directions for understanding polymer crystallization.

2019 ◽  
Author(s):  
Kyle Hall ◽  
Simona Percec ◽  
Michael Klein

This study reveals important features of polymer crystal formation at high-driving forces in entangled polymer melts based on simulations of polyethylene. First and in contrast to small-molecule crystallization, the heat released during polymer crystallization does not appreciably influence structural details of early-stage, crystalline clusters (crystal nuclei). Second, early-stage polymer crystallization (crystal nucleation) can occur without substantial chain-level relaxation and conformational changes. This study's results indicate that local structures and environments guide crystal nucleation in entangled polymer melts under high-driving force conditions. Given that such conditions are often used to process polyethylene, local structures and the separation of timescales associated with crystallization and chain-level processes are anticipated to be of substantial importance to processing strategies. This study highlights new research directions for understanding polymer crystallization.


2018 ◽  
Author(s):  
Kyle Hall ◽  
Simona Percec ◽  
Michael Klein

<p>This study reveals two important features of polymer crystal formation at high-driving forces in entangled polymer melts based on molecular dynamics simulations of polyethylene, a prototypical polymer. First, in contrast to existing literature on small-molecule crystallization, it is demonstrated that the heat released during polymer crystallization does not appreciably influence molecular-level structural details of early-stage, crystalline clusters (i.e., polymer crystal nuclei). Second, it is revealed that early-stage polymer crystallization (i.e., crystal nucleation) can occur without substantial chain-level relaxation and conformational changes, which is consistent with previous experimental work and yet in contrast to many previous computational studies. Given the conditions used to process polyethylene, the separation of timescales associated with crystallization and chain-level processes is anticipated to be of substantial importance to processing strategies. This study thus provides insights that highlight new research directions for understanding polymer crystallization under industrially-relevant conditions while also providing guidance as to how this work can be undertaken.</p>


2007 ◽  
Vol 40 (8) ◽  
pp. 2946-2954 ◽  
Author(s):  
Chen-Yang Liu ◽  
Roland Keunings ◽  
Christian Bailly

2007 ◽  
Vol 51 (3) ◽  
pp. 451-464 ◽  
Author(s):  
Fang Xu ◽  
Morton M. Denn ◽  
Jay D. Schieber

Polymers ◽  
2020 ◽  
Vol 12 (2) ◽  
pp. 447 ◽  
Author(s):  
Kyle Wm. Hall ◽  
Timothy W. Sirk ◽  
Simona Percec ◽  
Michael L. Klein ◽  
Wataru Shinoda

This study demonstrates that monodisperse entangled polymer melts crystallize via the formation of nanoscale nascent polymer crystals (i.e., nuclei) that exhibit substantial variability in terms of their constituent crystalline polymer chain segments (stems). More specifically, large-scale coarse-grain molecular simulations are used to quantify the evolution of stem length distributions and their properties during the formation of polymer nuclei in supercooled prototypical polyethylene melts. Stems can adopt a range of lengths within an individual nucleus (e.g., ∼1–10 nm) while two nuclei of comparable size can have markedly different stem distributions. As such, the attainment of chemically monodisperse polymer specimens is not sufficient to achieve physical uniformity and consistency. Furthermore, stem length distributions and their evolution indicate that polymer crystal nucleation (i.e., the initial emergence of a nascent crystal) is phenomenologically distinct from crystal growth. These results highlight that the tailoring of polymeric materials requires strategies for controlling polymer crystal nucleation and growth at the nanoscale.


2020 ◽  
Vol 53 (19) ◽  
pp. 8400-8405
Author(s):  
Brandon L. Peters ◽  
K. Michael Salerno ◽  
Ting Ge ◽  
Dvora Perahia ◽  
Gary S. Grest

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